510(k) K885247
K885247 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR". The FDA issued a decision of Substantially Equivalent on Mar 10, 1989. The device falls under product code LIT (Catheter, Angioplasty, Peripheral, Transluminal), a Class II device regulated under 21 CFR 870.1250. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 10, 1989
- Date Received
- Dec 22, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Catheter, Angioplasty, Peripheral, Transluminal
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type
- 510(k)